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Post Graduate Diploma in Monitoring of Clinical Trials
pharmaceutical business analytics distance course
Distance Learning
  • ✔ ACCRE USA Accredited
  • ✔ Program developed by senior industry experts
  • ✔ eBooks – Presentation & Notes on Cliniminds LMS
  • ✔ Cliniminds Certification after completion of program
  • ✔ MCQ based final exams
  • ✔ Introduction to Clinical Research & Phases of Clinical Trials | Indian Schedule Y & Other Guidelines | Ethical Considerations in Clinical Trials | Sponsor/Vendor Responsibilities | Essential Documents in Clinical Research | Protocol Writing | CRF Design | Site Selection Process | Pre-study Site Visits Monitoring | Site Initiation Monitoring | Routine Monitoring Visit | Case Report Form Review and Source Document Verification | Safety Reporting Monitoring | Study Drug Accountability Monitoring | Site Close-out Monitoring | Investigator Responsibilities | Informed Consent – Process & Documentation | Investigational Site Audits

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